[2H3]-Maprotiline hydrochloride

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Company Name: Artis Biotech Co. Ltd.  
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Products Intro: Product Name:Maprotiline D3 HCl
CAS:1329496-63-0
Purity:98% HPLC Package:5mg 20mg 50mg 100mg 200mg 1g
Company Name: Shanghai EFE Biological Technology Co., Ltd.  
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Products Intro: Product Name:Maprotiline-d3 HCl
CAS:1329496-63-0
Purity:95% Package:500μg;1mg;5mg
Company Name: Chengdu Novel Biomedical Co., Ltd.  
Tel: 028-85255396 18302801538
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Products Intro: Product Name:Maprotiline D3 HCl
CAS:1329496-63-0
Purity:98% HPLC Package:100mg;200mg
Company Name: Manhag Testing Technology Co., Ltd  
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Products Intro: Product Name:Maprotiline-[d3] hydrochloride
CAS:1329496-63-0
Purity:98.8 % Package:1mg
Company Name: ChemeGen 中国  
Tel: 18818260767
Email: sales@chemegen.com
Products Intro: Product Name:Maprotiline-d3 hydrochloride
CAS:1329496-63-0
Purity:98% Package:10 mg;50 mg;100 mg;500 mg;1 g;5 g;10 g
[2H3]-Maprotiline hydrochloride Basic information
Product Name:[2H3]-Maprotiline hydrochloride
Synonyms:[2H3]-Maprotiline hydrochloride;Maprotiline-d3 HCl;Maprotiline hydrochloride salt;N-methyl-d3-9,10-ethanoanthracene-9(10H)-propanamine, monohydrochloride
CAS:1329496-63-0
MF:C20H24ClN
MW:313.87
EINECS:
Product Categories:
Mol File:1329496-63-0.mol
[2H3]-Maprotiline hydrochloride Structure
[2H3]-Maprotiline hydrochloride Chemical Properties
storage temp. -20°C
solubility DMSO: soluble,Methanol: soluble
form A solid
color White to off-white
Safety Information
MSDS Information
[2H3]-Maprotiline hydrochloride Usage And Synthesis
Biological ActivityMaprotiline-d3 is intended for use as an internal standard for the quantification of maprotiline by GC- or LC-MS. Maprotiline is a tricyclic antidepressant.1,2 It binds to the norepinephrine transporter (NET; Kd = 11 nM) and is selective for NET over the serotonin and dopamine transporters (Kds = 5,800 and 1,000 nM, respectively).2 Maprotiline also binds to the serotonin (5-HT) receptor subtype 5-HT2A (Ki = 51 nM), as well as histamine H1, muscarinic acetylcholine, α1-adrenergic, and dopamine D2 receptors (Kds = 2, 570, 90, and 350 nM, respectively).3 In vivo, maprotiline inhibits norepinephrine reuptake in rat brain and peripheral tissues.4 It reduces isolation-induced aggressive behavior and inhibits electrical foot-shock stimulation-induced belligerence in mice when administered at doses ranging from 3 to 10 mg/kg. Maprotiline also reduces aggressive behavior in rhesus monkeys housed in groups. Formulations containing maprotiline have been used in the treatment of depression and anxiety.
References1.Spencer, P.S.Review of the pharmacology of existing antidepressantsBr. J. Clin. Pharmacol.4(Suppl 2)57S-68S(1977) 2.Tatsumi, M., Groshan, K., Blakely, R.D., et al.Pharmacological profile of antidepressants and related compounds at human monoamine transportersEur. J. Pharmacol.340(2-3)249-258(1997) 3.Richelson, E., and Nelson, A.Antagonism by antidepressants of neurotransmitter receptors of normal human brain in vitroJ. Pharmacol. Exp. Ther.230(1)94-102(1984) 4.Pinder, R.M., Brogden, R.N., Speight, T.M., et al.Maprotiline: A review of its pharmacological properties and therapeutic efficacy in mental depressive statesDrugs13(5)321-352(1977)
[2H3]-Maprotiline hydrochloride Preparation Products And Raw materials
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